The mouse Pol I terminator is more efficient than the hepatitis delta virus ribozyme in generating influenza-virus-like RNAs with precise 3' ends in a plasmid-only-based virus rescue system

被引:11
作者
Feng, Liqiang [1 ,2 ]
Li, Feng [1 ]
Zheng, Xuehua [1 ]
Pan, Weiqi [1 ]
Zhou, Kai [2 ,3 ]
Liu, Yichu [1 ]
He, Hongxuan [3 ]
Chen, Ling [1 ]
机构
[1] Chinese Acad Sci, Ctr Vaccines & Biotherapeut, Guangzhou Inst Biomed & Hlth, Guangzhou 510663, Guangdong, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Key Lab Anim Ecol & Conservat Biol, Natl Res Ctr Wildlife Born Dis, Inst Zool, Beijing 100101, Peoples R China
关键词
REVERSE GENETICS SYSTEM; A VIRUS; PACKAGING SIGNALS; SEGMENTS; VIRIONS; REGIONS; GENES; VRNA; DNA;
D O I
10.1007/s00705-009-0422-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Reverse genetics systems for generating recombinant influenza viruses are based on two different mechanisms for obtaining the 3' end of the viral RNA: one uses the self-cleaving hepatitis delta virus ribozyme (HDVR), and the other uses the murine RNA polymerase I (Pol I) terminator. In this study, we employed EGFP and Renilla luciferase reporter constructs to compare the efficiency of both methods. Our results indicate that the murine Pol I terminator was more efficient than the HDVR, which will be helpful in choosing an influenza virus rescue system, as well as in establishing other RNA virus rescue systems.
引用
收藏
页码:1151 / 1156
页数:6
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